US4614742A - Fluorinated isophthalonitrile compound and nonmedical fungicide containing the same - Google Patents
Fluorinated isophthalonitrile compound and nonmedical fungicide containing the same Download PDFInfo
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- US4614742A US4614742A US06/770,481 US77048185A US4614742A US 4614742 A US4614742 A US 4614742A US 77048185 A US77048185 A US 77048185A US 4614742 A US4614742 A US 4614742A
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- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
- C07D239/46—Two or more oxygen, sulphur or nitrogen atoms
- C07D239/47—One nitrogen atom and one oxygen or sulfur atom, e.g. cytosine
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- A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
- A01N37/36—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing at least one carboxylic group or a thio analogue, or a derivative thereof, and a singly bound oxygen or sulfur atom attached to the same carbon skeleton, this oxygen or sulfur atom not being a member of a carboxylic group or of a thio analogue, or of a derivative thereof, e.g. hydroxy-carboxylic acids
- A01N37/38—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing at least one carboxylic group or a thio analogue, or a derivative thereof, and a singly bound oxygen or sulfur atom attached to the same carbon skeleton, this oxygen or sulfur atom not being a member of a carboxylic group or of a thio analogue, or of a derivative thereof, e.g. hydroxy-carboxylic acids having at least one oxygen or sulfur atom attached to an aromatic ring system
- A01N37/40—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing at least one carboxylic group or a thio analogue, or a derivative thereof, and a singly bound oxygen or sulfur atom attached to the same carbon skeleton, this oxygen or sulfur atom not being a member of a carboxylic group or of a thio analogue, or of a derivative thereof, e.g. hydroxy-carboxylic acids having at least one oxygen or sulfur atom attached to an aromatic ring system having at least one carboxylic group or a thio analogue, or a derivative thereof, and one oxygen or sulfur atom attached to the same aromatic ring system
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- A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
- A01N37/44—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing at least one carboxylic group or a thio analogue, or a derivative thereof, and a nitrogen atom attached to the same carbon skeleton by a single or double bond, this nitrogen atom not being a member of a derivative or of a thio analogue of a carboxylic group, e.g. amino-carboxylic acids
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- A01N39/00—Biocides, pest repellants or attractants, or plant growth regulators containing aryloxy- or arylthio-aliphatic or cycloaliphatic compounds, containing the group or, e.g. phenoxyethylamine, phenylthio-acetonitrile, phenoxyacetone
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- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
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- A01N43/06—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom five-membered rings
- A01N43/08—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom five-membered rings with oxygen as the ring hetero atom
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- A—HUMAN NECESSITIES
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- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
- A01N43/50—1,3-Diazoles; Hydrogenated 1,3-diazoles
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- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
- A01N43/50—1,3-Diazoles; Hydrogenated 1,3-diazoles
- A01N43/52—1,3-Diazoles; Hydrogenated 1,3-diazoles condensed with carbocyclic rings, e.g. benzimidazoles
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- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
- A01N43/54—1,3-Diazines; Hydrogenated 1,3-diazines
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- A—HUMAN NECESSITIES
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- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/64—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with three nitrogen atoms as the only ring hetero atoms
- A01N43/647—Triazoles; Hydrogenated triazoles
- A01N43/653—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
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- C07C255/00—Carboxylic acid nitriles
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- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C323/00—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups
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- C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
- C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D231/12—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
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- C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
- C07D233/56—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, attached to ring carbon atoms
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- C07D235/02—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings condensed with carbocyclic rings or ring systems
- C07D235/04—Benzimidazoles; Hydrogenated benzimidazoles
- C07D235/24—Benzimidazoles; Hydrogenated benzimidazoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached in position 2
- C07D235/30—Nitrogen atoms not forming part of a nitro radical
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- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
- C07D239/46—Two or more oxygen, sulphur or nitrogen atoms
- C07D239/52—Two oxygen atoms
- C07D239/54—Two oxygen atoms as doubly bound oxygen atoms or as unsubstituted hydroxy radicals
- C07D239/545—Two oxygen atoms as doubly bound oxygen atoms or as unsubstituted hydroxy radicals with other hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
- C07D239/553—Two oxygen atoms as doubly bound oxygen atoms or as unsubstituted hydroxy radicals with other hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms with halogen atoms or nitro radicals directly attached to ring carbon atoms, e.g. fluorouracil
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- C07D249/00—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
- C07D249/02—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms not condensed with other rings
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- C07D249/00—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
- C07D249/02—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms not condensed with other rings
- C07D249/08—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
- C07D249/10—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D249/14—Nitrogen atoms
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- C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
- C07D307/02—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings
- C07D307/04—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having no double bonds between ring members or between ring members and non-ring members
- C07D307/10—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having no double bonds between ring members or between ring members and non-ring members with substituted hydrocarbon radicals attached to ring carbon atoms
- C07D307/12—Radicals substituted by oxygen atoms
Definitions
- the present invention relates to a novel fluorinated isophthalonitrile compound suitable for use as an agricultural fungicide or germicide as well as antibacterial and mildewproofing agent for various industrial products and the raw materials thereof.
- the present invention also relates to a nonmedical fungicide.
- the objects of the present invention are to provide novel compounds having the above-mentioned desired antibacterial and mildewproofing effects and having excellent agricultural fungicidal properties.
- nonmedical fungicide comprising, as an effective ingredient, the fluorinated isophthalonitrile having the above-mentioned general formula (I).
- novel fluorinated isophthalonitrile compounds having the above-mentioned general formula (I). Typical examples of such compounds are shown in Table 1.
- the fluorinated isophthalonitrile compounds having the general formula (I) according to the present invention can be prepared as follows. ##STR32## wherein Y and R are the same as defined above.
- the starting materials (II) and (III) are mixed to allow to be reacted in the presence or absence of a solvent to form the desired fluorinated isophthalonitrile compounds (I).
- the reaction is preferably carried out at a temperature between -20° C. and the reflux temperature of a solvent.
- the starting material (III) may be used as a reaction solvent.
- aprotic solvents such as acetonitrile, chloroform, dichloromethane, benzene, toluene, dioxane, ethyl ether, tetrahydrofuran, and ethyl acetate may be used as a reaction solvent.
- the above-mentioned reaction can be advantageously accelerated when a catalytic amount, or an amount equimolecular to 10 times the starting material (II), of a base such as an alkali hydroxide, triethylamine, pyridine, an alkali carbonate, or potassium fluoride is used.
- a base such as an alkali hydroxide, triethylamine, pyridine, an alkali carbonate, or potassium fluoride is used.
- the starting compound (II), i.e., tetrafluoroisophthalonitrile, can be prepared from tetrachloroisophthalonitrile in a known manner (see, for example, British Pat. No. 1026290 (1966), Bull. Chem. Soc. Japan 40, 688 (1966), Kagaku Kogyo Zasshi (Japan) 73, 447 (1970), and Japanese Examined Patent Publication No. 41-11358).
- the fluorinated isophthalonitrile compounds according to the present invention have excellent and remarkable mildewproofing action and antibacterial action and also have wide action spectra and are very stable against ultraviolet light. Furthermore, when the fluorinated isophthalonitrile compounds according to the present invention are used as an agricultural fungicide in the field or as an industrial antibacterial and mildewproofing agent outdoors, the compounds exhibit excellent prolonged activity.
- the nonmedical fungicides according to the present invention contain, as an effective or active ingredient, one or more of the above-mentioned fluorinated isophthalonitrile compounds, preferably in an amount of 1% to 95% by weight, more preferably 10% to 80% by weight, of the total amount of the composition.
- the present fungicide has excellent curative effects (i.e., effects obtained by directly applying the present agent to the portion where harmful fungi or bacteria are generated) and excellent preventive effects (i.e., effects obtained by applying the present agent to the portion where harmful fungi or bacteria are expected to be generated).
- the above-mentioned effective compounds according to the present invention can be directly used as a nonmedical fungicide.
- the present compounds can be formulated with bases to form various forms of preparations such as powder, wettable powder, tablets, oily agents, gaseous agents, emulsions, aerosols, and fumigants.
- bases usable in the formulation of the present fungicides may be in the form of solid, liquid, or gas.
- the solid bases usable in the present invention are talc, clay, kaolin, diatomaceous earth, calcium carbonate, potassium chlorate, silica, niter, woodmeal, nitrocellulose, starch, wheat flour, soybean flour, and gum arabic.
- liquid bases usable in the present invention are water and organic solvents.
- organic solvents are hydrocarbons such as benzene, toluene, xylene, kerosine, diesel oil, fuel oil, petroleum, and naphtha; ketones such as acetone, methylethyl ketone, and cyclohexanone; chlorinated hydrocarbons such as carbon tetrachloride, chloroform, trichloroethylene, and perchloroethylene; amyl acetate and butyl acetate; monoalkyl ethers, e.g., monomethyl ether and monoethyl ether, of ethylene glycol; and alcohols such as methanol, ethanol, isopropanol, and amyl alcohol.
- hydrocarbons such as benzene, toluene, xylene, kerosine, diesel oil, fuel oil, petroleum, and naphtha
- ketones such as acetone, methylethyl ket
- gaseous bases usable in the present invention are air, nitrogen, carbon dioxide, Freon (registered trademark of DuPont for fluorohydrocarbons), propane, and butane.
- nonionic, anionic, cationic, or ampholytic surfactants can be used as an adjuvant (i.e., a wetting agent, emulsifier, dispersing agent, spreader).
- the nonmedical germicides according to the present invention are effective for controlling a wide variety of diseases of various agricultural and garden crops and are also effective against microorganisms, such as fungi, algae, bacteria, and organisms of slime, which adversely affect industrial products or the starting materials thereof.
- microorganisms such as fungi, algae, bacteria, and organisms of slime, which adversely affect industrial products or the starting materials thereof. Examples of such diseases and microorganisms are as follows.
- Rhizopus spp. Rhizopus spp., Gliocladium spp.,
- Myrothecium spp. Rhodotorula spp., and
- the nonmedical fungicide according to the present invention can be preferably used in a concentration of 1 to 1000 ppm, more preferably 10 to 500 ppm, in the formulated composition, although the concentration of the active component depends upon the kinds of diseases and microorganisms.
- the above-mentioned diseases can be effectively controlled and industrial products and the raw materials thereof can be advantageously, protected from damages caused by various microorganisms.
- the germicide according to the present invention can be used alone in the preparations thereof. It should be noted, however, that the active component of the present germicide can also be formulated into the preparations together with one or more agents such as various conventional insecticides, bactericides, fungicides, herbicides, plant growth regulators miticides, nematocides, attractants, repellents, nutrients, fertilizers, and soil structure conditioning agents. Thus, these preparations are expected to exhibit various wide effects.
- the nonmedical fungicides can be used as a fungicide, in addition to the above-mentioned agricultural and garden fungicides, for preventing the industrial products and the raw materials thereof from adverse effects or damage caused by various microorganisms.
- industrial products and the raw materials thereof are plastics, plasters, carpets, adhesives, emulsions (or emulsified liquids), paints, coating agents, hides, glues, wood (or timbers), fibers, paper, and cardboard.
- the present fungicides can be similarly applied to the portions of industrial plants such as cooling water circulation system and cooling lubricating oil circulation system.
- the desired compound was prepared in the same manner as in Synthetic Example 2 by using diethyl amine in lieu of the aniline.
- the resultant yellow liquid was distilled in vacuo to obtain 2.0 g (91% yield) of the desired compound No. 14 as a fraction at a boiling point of 144° C. to 146° C./7 mmHg.
- the desired compound was obtained in the same manner as in Synthetic Example 5, except that ethanol was used in lieu of methanol. The yield was 90%.
- the desired compound was obtained in the same manner as in Synthetic Example 5, except that isopropanol was used in lieu of methanol.
- the yield was 86%.
- a 2.0 g amount of tetrafluoroisophthalonitrile and 0.87 g of potassium fluoride were dissolved in 10 ml of acetonitrile. After cooling the mixture to a temperature of 0° C. by an ice-water bath, 1.1 g of phenyl mercaptan was dropwise added by a syringe. While mixture was maintained at a temperature of about 0° C., the mixture was stirred for 8 hours and the solvent was then distilled off. A 50 ml amount of water was added to the mixture and potassium fluoride was dissolved. The mixture was extracted with chloroform, and the extract was dried with magnesium sulfate.
- the desired compound was obtained in the same manner as in Synthetic Example 11, except that allyl alcohol was used in lieu of methallyl alcohol.
- the desired compound was prepared in the same manner as in Synthetic Example 17, except that the isopropylmercaptan was used in lieu of n-propylmercaptan. Thus, 1.6 g (63% yield) of the desired compound No. 51 was obtained.
- the desired compound was obtained in the same manner as in Synthetic Example 19, except that isobutylmercaptan was used in lieu of n-butylmercaptan.
- Powder germicides having the following compositions were prepared by mixing the ingredients listed below at room temperature.
- Wettable powder germicides having the following compositions were prepared by mixing the ingredients listed below at room temperature.
- a filter paper having a diameter of 8 mm which was prepared by absorbing a certain amount of the active compound, followed by air drying, was placed on the plate. After 48 hour incubation, the diameter of the inhibited circle was measured. Two tests were carried out in each run.
- a sample agent diluted to a certain concentration was uniformly sprayed on the developed leaves of pear trees (variety: Nijyusseiki) in an amount of 20 ml per 5 leaves and was dried in a room.
- a sample liquid agent containing a certain amount of an active compound was uniformly sprayed on rice seedlings (variety: Jyukkoku) at true leaf stage in a pot with the volume of 200 liter/10 a and was air-dried in a green house.
- a spore suspension previously prepared in such a way that 40 conidia of rice blast fungus were present in a visual area of a 100 magnification microscope was uniformly sprayed and inoculated.
- the sprayed rice seedlings were allowed to stand under dark conditions of a temperature of 23° C. and a relative humidity of 100%.
- the rice seedlings were transferred to a green house and, after 10 days from the inocuration, the degree of the infection was determined.
- the inhibition value was calculated as follows. Three tests were carried out in each run. ##EQU1## wherein n: Number of leaves in each infection degree
- Test Example 3 was repeated except that the active compound was changed.
- a 10 ml amount of a potato-agar medium containing a certain concentration of each active ingredient was poured into a petri dish. After solidifying, a spore suspension of each test microorganism having 2.00 to 3.00 ⁇ 10 6 spores/ml was inoculated in the form of streaks with a platinum loop amount. The petri dish was allowed to stand in a constant temperature room at 25° C. for 3 days. Thereafter, the degree of growth was examined and the minimum inhibition concentration (i.e., "MIC") was determined. Four tests were carried out in each run.
- MIC minimum inhibition concentration
- a 10 ml amount of a potato-agar medium containing a certain concentration of each active ingredient was poured into a petri dish. After solidifying, the tip portion of the flora of each test microorganism previously incubated on a plate culture medium, which was punched with a 8 cm ⁇ cork borer, was inoculated in the active ingredient containing culture medium. The culture medium thus obtained was allowed to stand in a constant temperature room at 28° C. for 3 days. Therefore, the growth of the microorganism was examined and the MIC was determined. Four tests were carried out in each run.
- a 10 ml amount of a normal bouillon-agar culture medium was poured into a petri dish. After solidifying, a bacterial suspension previously obtained from the cultivation in the same liquid medium was inoculated in the form of streaks with a platinum loop amount. The petri dish was allowed to stand for 2 days in a constant temperature room at 30° C. Thereafter, the growth of the microorganism was examined and the MIC was determined. Four tests were carried out in each run.
- the rhizome portion of Japanese raddish was cut to the form of a ring having a thickness of 1 cm with a 18 cm ⁇ cork borer to form raddish chips.
- the chips were dipped in a liquid containing a certain concentration of an active ingredient for one hour. After air drying, one drop of a culture liquid containing bacterial soft rot bacteria which was cultivated at 27° C. for 24 hours in a normal bouillon medium by shaking culture, was inoculated in the center of the raddish chip.
- the raddish chip was allowed to stand at a temperature of 27° C. for 2 days under a high humidity condition. Therefore, the putrefaction degree of the raddish chip was examined. Five tests were carried out in each run.
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- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
A fluorinated isophthalonitrile compound having the general formula ##STR1## wherein Y is --O, --S, or --N(R'), R and R' are independently hydrogen, an alkyl group, an alkyl group, an alkynyl group, a haloalkyl group, an alkoxyl group, alkoxyalkyl group, a phenyl group which may be substituted, a tetrahydrofurfuryl group, or a cycloalkyl group, provided that, in the case of Y=--N(R'), R and R' or Y may be a tetrahydrofurfuryl group, or a cycloalkyl group, a heterocyclic compound residue.
This fluorinated isophthalonitrile compound is suitable for use as an agricultural fungicide.
Description
1. Field of the Invention
The present invention relates to a novel fluorinated isophthalonitrile compound suitable for use as an agricultural fungicide or germicide as well as antibacterial and mildewproofing agent for various industrial products and the raw materials thereof. The present invention also relates to a nonmedical fungicide.
2. Description of the Related Art
It is heretofore known, as shown in, for example, Japanese Examined Patent Publication (Kokoku) No. 41-11358, that halogenated aromatic dinitriles have biological activities suitable for use as a fungicide, a bactericide, a nematocide, and a herbicide. 4-Alkoxy-2,5,6-trichloroisophthalonitrile compounds are also known as a mildewproofing agent as shown in, for example, Japanese Unexamined Patent Publication (Kokai) No. 50-121424. Furthermore, it has recently become problems that various industrial products and the raw materials thereof are damaged by microorganisms such as bacteria, fungi, and yeasts. These damages not only detract from the external appearance and health and sanitary properties, but also detrimentally affect performance and qualities. In order to prevent these damages, it is strongly desired in the art to develop antibacterial and mildewproofing agent having large antibacterial and mildewproofing effects, wide antibacterial spectra, and other properties depending upon the usage thereof (e.g., water resistance, heat resistance, light resistance, decomposability, and stability).
Accordingly, the objects of the present invention are to provide novel compounds having the above-mentioned desired antibacterial and mildewproofing effects and having excellent agricultural fungicidal properties.
Other objects and advantages of the present invention will be apparent from the following description.
In accordance with the present invention, there is provided a fluorinated isophthalonitrile compound having the general formula ##STR2## wherein Y is --O, --S, or --N(R'), R and R' and independently hydrogen, an alkyl group, preferably having 1 to 10 carbon atoms, an alkenyl group, preferably having 3 to 10 carbon atoms, an alkynyl group, preferably having 3 to 10 carbon atoms a haloalkyl group preferably having 1 to 10 carbon atoms, an alkoxyl group, preferably having 1 to 10 carbon atoms, an alkoxyalkyl group, preferably having 2 to 10 carbon atoms, a phenyl group which may be substituted, a tetrahydrofurfuryl group, or a cycloalkyl group, preferably having 3 to 8 carbon atoms, provided that, in the case of Y=-N(R'), R and R' or Y may be a heterocyclic compound residue, preferably pyrazol-3-yl, 1,2,4-triazol-3-yl, benzimidazol-2-yl, 2(1H)-pyrimidinon-6-yl, imidazol-1-yl, pyrazol-1-yl, pyrimidine-2,4(1H,3H)-dion-1-yl, morpholino, piperidino group which may be substituted.
In accordance with the present invention, there is also provided a nonmedical fungicide comprising, as an effective ingredient, the fluorinated isophthalonitrile having the above-mentioned general formula (I).
According to the present invention, there is provided novel fluorinated isophthalonitrile compounds having the above-mentioned general formula (I). Typical examples of such compounds are shown in Table 1.
TABLE 1
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Physical Property
Com- Melting point (mp),
pound YR in Boiling point (bp),
No. formula (I) Refractive index (n.sub.D)
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1 NH.sub.2 mp 191-193° C.
2 NHCH.sub.3 mp 107-109° C.
3 NHC.sub.2 H.sub.5
mp 75-77° C.
4 NHC.sub.4 H.sub.9-n
bp 165-167° C./2.5 mmHg
5 N(C.sub.4 H.sub.9-n).sub.2
bp 137-139° C./2.5 mmHg
##STR3## mp 131.5-134° C.
7
##STR4## mp 167° C.
8
##STR5## mp 158° C.
9
##STR6## mp 260° C.
10
##STR7## mp 260° C. or more
11
##STR8## mp 260° C. or more
12
##STR9## mp 64-66° C.
13
##STR10## mp 190-191° C.
14 N(C.sub.2 H.sub.5).sub.2
bp 144-146° C./7 mmHg
15
##STR11## mp 209-210° C.
16
##STR12## mp 260° C. or more
17
##STR13## mp 211° C.
18
##STR14## mp 138-139° C.
19 OH mp 168-172° C.
20 OCH.sub.3 mp 71-72° C.
21 OC.sub.2 H.sub.5 mp 59-62° C.
22 SC.sub.2 H.sub.5 n.sub.D.sup.18.5 1.5610
bp 115-118° C./0.3 mmHg
23 On-C.sub.3 H.sub.2
mp 54-56° C.
24 Oi-C.sub.3 H.sub.7
mp 63-64° C.
25 On-C.sub.4 H.sub.9
bp 134-136° C./0.3 mmHg
26 Oi-C.sub.4 H.sub.8
bp 121-123° C./0.3 mmHg
27 OCH.sub.2 CHCH.sub.2
mp 50° C. or less,
n.sub.D.sup.30 1.5136
28 OCF.sub.3 CH.sub.2
n.sub.D.sup.27 1.4635
29
##STR15## mp 81-85° C.
30
##STR16## mp 119-121° C.
31
##STR17## mp 55° C. or less
32
##STR18## mp 99-101° C.
33
##STR19## mp 96-98° C.
34
##STR20## n.sub.D.sup.26 1.5608
35
##STR21## mp 55° C. or less
36
##STR22## mp 88-91° C.
37
##STR23## mp 110-115° C.
38
##STR24## mp 55° C. or less
39
##STR25## mp 84° C.
40
##STR26## mp 90-95° C.
41
##STR27## mp 90-92° C. bp 65-67° C./0.7 mmHg
42
##STR28## mp 50° C. or less
43 OCH.sub.2 CH.sub.2 OCH.sub.3
n.sub.D.sup.24 1.5030
44
##STR29## n.sub.D.sup.24 1.5186
45 On-C.sub.6 H.sub.13
n.sub.D.sup.24 1.4937
46 On-C.sub.8 H.sub.17
n.sub.D.sup.24 1.4906
47
##STR30## n.sub.D.sup.24 1.5036
48
##STR31## bp 113° C./0.21 mmHg
49 SCH.sub.3 mp 50° C. or less,
n.sub.D.sup.40 1.5651
50 Sn-C.sub.3 H.sub.7
mp 50° C. or less,
n.sub.D.sup.40 1.5524
51 Siso-C.sub.3 H.sub.7
mp 50° C. or less,
n.sub.D.sup.40 1.5495
52 Sn-C.sub.4 H.sub.9
bp 138-139° C./0.3 mmHg,
n.sub.D.sup.28 1.5486
53 Siso-C.sub.4 H.sub.9
bp 120-121° C./0.18 mmHg,
n.sub.D.sup.28 1.5403
54 Ssec-C.sub.4 H.sub.9
bp 106-108° C./0.15 mmHg,
n.sub.D.sup.40 1.5440
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The fluorinated isophthalonitrile compounds having the general formula (I) according to the present invention can be prepared as follows. ##STR32## wherein Y and R are the same as defined above.
Thus, the starting materials (II) and (III) are mixed to allow to be reacted in the presence or absence of a solvent to form the desired fluorinated isophthalonitrile compounds (I). The reaction is preferably carried out at a temperature between -20° C. and the reflux temperature of a solvent. The starting material (III) may be used as a reaction solvent. Alternatively, aprotic solvents such as acetonitrile, chloroform, dichloromethane, benzene, toluene, dioxane, ethyl ether, tetrahydrofuran, and ethyl acetate may be used as a reaction solvent. Furthermore, the above-mentioned reaction can be advantageously accelerated when a catalytic amount, or an amount equimolecular to 10 times the starting material (II), of a base such as an alkali hydroxide, triethylamine, pyridine, an alkali carbonate, or potassium fluoride is used.
The starting compound (II), i.e., tetrafluoroisophthalonitrile, can be prepared from tetrachloroisophthalonitrile in a known manner (see, for example, British Pat. No. 1026290 (1966), Bull. Chem. Soc. Japan 40, 688 (1966), Kagaku Kogyo Zasshi (Japan) 73, 447 (1970), and Japanese Examined Patent Publication No. 41-11358).
The fluorinated isophthalonitrile compounds according to the present invention have excellent and remarkable mildewproofing action and antibacterial action and also have wide action spectra and are very stable against ultraviolet light. Furthermore, when the fluorinated isophthalonitrile compounds according to the present invention are used as an agricultural fungicide in the field or as an industrial antibacterial and mildewproofing agent outdoors, the compounds exhibit excellent prolonged activity.
The nonmedical fungicides according to the present invention contain, as an effective or active ingredient, one or more of the above-mentioned fluorinated isophthalonitrile compounds, preferably in an amount of 1% to 95% by weight, more preferably 10% to 80% by weight, of the total amount of the composition. Thus, the present fungicide has excellent curative effects (i.e., effects obtained by directly applying the present agent to the portion where harmful fungi or bacteria are generated) and excellent preventive effects (i.e., effects obtained by applying the present agent to the portion where harmful fungi or bacteria are expected to be generated).
The above-mentioned effective compounds according to the present invention can be directly used as a nonmedical fungicide. Furthermore, the present compounds can be formulated with bases to form various forms of preparations such as powder, wettable powder, tablets, oily agents, gaseous agents, emulsions, aerosols, and fumigants.
These bases usable in the formulation of the present fungicides may be in the form of solid, liquid, or gas. Examples of the solid bases usable in the present invention are talc, clay, kaolin, diatomaceous earth, calcium carbonate, potassium chlorate, silica, niter, woodmeal, nitrocellulose, starch, wheat flour, soybean flour, and gum arabic.
Examples of the liquid bases usable in the present invention are water and organic solvents. Typical examples of the organic solvents are hydrocarbons such as benzene, toluene, xylene, kerosine, diesel oil, fuel oil, petroleum, and naphtha; ketones such as acetone, methylethyl ketone, and cyclohexanone; chlorinated hydrocarbons such as carbon tetrachloride, chloroform, trichloroethylene, and perchloroethylene; amyl acetate and butyl acetate; monoalkyl ethers, e.g., monomethyl ether and monoethyl ether, of ethylene glycol; and alcohols such as methanol, ethanol, isopropanol, and amyl alcohol.
Examples of the gaseous bases usable in the present invention are air, nitrogen, carbon dioxide, Freon (registered trademark of DuPont for fluorohydrocarbons), propane, and butane.
In addition to the above-mentioned bases, various conventional ingredients can be optionally incorporated into the present germicide. For example, nonionic, anionic, cationic, or ampholytic surfactants can be used as an adjuvant (i.e., a wetting agent, emulsifier, dispersing agent, spreader).
The nonmedical germicides according to the present invention are effective for controlling a wide variety of diseases of various agricultural and garden crops and are also effective against microorganisms, such as fungi, algae, bacteria, and organisms of slime, which adversely affect industrial products or the starting materials thereof. Examples of such diseases and microorganisms are as follows.
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Group I (Diseases)
Crops Diseases
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Rice Blast
Brown spot
Sheath blight
Bacterial leaf blight
Wheat Spot blotch
Snow mold
Typhula snow blight
Potato Late blight
Early blight
Black scurf
Pulse Brown spot
Frog-eye leaf spot
Downy mildew
Stem rot
Tobacco Wild fire
Black shank
Tea Bacterial shoot blight
Blister blight
Net blister blight
Anthracnose
Gray blight
Sugar beet Downy mildew
Cercospora leaf spot
Damping-off
Tomato Bacterial canker
Late blight
Gray mold
leaf mold
Fusarium wilt
Stem rot
Damping-off
Early blight
Cucumber Gray mold
Downy mildew
Phytophthora rot
Scab
Damping-off
Anthracnose
Gummy stem blight
Fusarium wilt
Japanese raddish Black rot
(daikon) Bacterial soft rot
Yellows (wilt)
Gray leaf spot
(Alternaria leaf spot)
Downy mildew
Onion Bacterial soft rot
Downy mildew
Gray-mold neck rot
Lettuce Bacterial soft rot
Stem rot
Citrus fruit Gray mold
Canker
Melanose
Scab
Apple Blossom blight
Scab
Alternaria leaf spot
Japanese persimmon Gray mold
(kaki) Circular leaf spot
Angular leaf spot
Anthracnose
Japanese pear Scab
Black spot
Peach Brown rot
Scab
Phomopsis rot
Bacterial shot hole
Grape Downy mildew
Anthracnose
Gray mold
Ripe rot
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Bacillus spp., Staphylococcus spp.,
Escherichia spp., Pseudomonas spp.,
Serratia spp., Alternaria spp.,
Aspergillus spp., Penicillium spp.,
Cladosporium spp., Mucor spp.,
Rhizopus spp., Gliocladium spp.,
Eurotium spp., Aureobasidium spp.,
Chaetomium spp., Fusarium spp.,
Myrothecium spp., Rhodotorula spp., and
Saccharomyces spp.
The nonmedical fungicide according to the present invention can be preferably used in a concentration of 1 to 1000 ppm, more preferably 10 to 500 ppm, in the formulated composition, although the concentration of the active component depends upon the kinds of diseases and microorganisms. Thus, the above-mentioned diseases can be effectively controlled and industrial products and the raw materials thereof can be advantageously, protected from damages caused by various microorganisms.
The germicide according to the present invention can be used alone in the preparations thereof. It should be noted, however, that the active component of the present germicide can also be formulated into the preparations together with one or more agents such as various conventional insecticides, bactericides, fungicides, herbicides, plant growth regulators miticides, nematocides, attractants, repellents, nutrients, fertilizers, and soil structure conditioning agents. Thus, these preparations are expected to exhibit various wide effects.
The nonmedical fungicides can be used as a fungicide, in addition to the above-mentioned agricultural and garden fungicides, for preventing the industrial products and the raw materials thereof from adverse effects or damage caused by various microorganisms. Examples of such industrial products and the raw materials thereof are plastics, plasters, carpets, adhesives, emulsions (or emulsified liquids), paints, coating agents, hides, glues, wood (or timbers), fibers, paper, and cardboard. Further, the present fungicides can be similarly applied to the portions of industrial plants such as cooling water circulation system and cooling lubricating oil circulation system.
The present invention will be further explained by, but is by no means limited to, the following Synthetic Examples, Formulation Examples, and Test Examples. In Synthetic Examples, 19 Fnmr and 1 Hnmr are the NMR data determined by using trifluoro acetic acid as an outer standard and tetramethyl silane as an inner standard, respectively, unless otherwise specified.
To a solution of 2.0 g of tetrafluoroisophthalonitrile in 20 ml of acetonitrile, 0.6 ml of 28% aqueous ammonia was dropwise added. After the dropwise addition, the mixture was stirred at room temperature for one hour. An aqueous sodium bicarbonate solution was added to the mixture and the resultant mixture was extracted with chloroform and was washed with an aqueous sodium chloride solution. After drying with sodium sulfate, the chloroform was distilled off to obtain yellow crystal. The resultant crystal was recrystallized from chloroform to obtain 1.2 g (61% yield) of the desired compound No. 1.
The analytical results are as follows.
19 Fnmr (CCl4 /DMSOd6) δ25.0 (d,JFF =9.4 Hz, 1F) 46.7 (d, JFF =18.8 Hz, 1F) 80.0 (dd, JFF =18.8 Hz, 9.4 Hz, 1F).
1 Hnmr (CCl4 /DMSOd6) δ2.8 (s).
A solution of 0.85 g of aniline in 20 ml of acetonitrile was dropwise added, while stirring, to a solution of 2.0 g of tetrafluoroisophthalonitrile and 2.0 g of triethylamine in 30 ml of acetonitrile. After dropwise adding, the mixture was stirred at room temperature for 1 hour and an aqueous sodium bicarbonate solution was then added. The mixture was extracted with chloroform and the chloroform extract was washed 5 times with an aqueous sodium chloride solution. After drying with magnesium sulfate, the chloroform was distilled off. The resultant crude crystal was purified by silica gel chromatography (solvent:hexane). Thus, 2.3 g (87% yield) of the desired compound No. 6 was obtained.
The analytical results are as follows.
19 Fnmr (CCl4 /DMSOd6) δ24.3 (d, JFF =9.4 Hz, 1F); 45.4 (d, JFF =19.0 Hz, 1F); 72.7 (dd, JFF =19.0 Hz, 9.4 Hz, 1F).
1 Hnmr (CCl4 /DMSOd6) δ3.7 (s, 1H), 7.4 (s, 5H).
The desired compound was prepared in the same manner as in Synthetic Example 2 by using diethyl amine in lieu of the aniline. The resultant yellow liquid was distilled in vacuo to obtain 2.0 g (91% yield) of the desired compound No. 14 as a fraction at a boiling point of 144° C. to 146° C./7 mmHg.
The analytical results are as follows.
19 Fnmr (CCl4 /DMSO-d6) δ23.4 (dd, JFF =9 Hz, 1.8 Hz, 1F) 43.2 (dd, JFF =18 Hz, 1.8 Hz, 1F) 69.5 (ddd, JFF =18 Hz, 9 Hz, 1F).
1 Hnmr (CCl4 /DMSO-d6) δ1.2 (t, 3H); 3.4 (q, 2H).
A 2.0 g amount of tetrafluoroisophthalonitrile and 0.7 g of sodium hydroxide were added to 40 ml of water and the mixture was heated under reflux for 1.5 hours. After cooling, the mixture was neutralized with concentrated hydrochloric acid and was then extracted with ether. After the ether extract was washed with water, the extract was dried with magnesium sulfate. The solvent was distilled off and the resultant crude crystal was recrystallized to obtain 1.39 g of the desired compound No. 19.
The analytical results are as follows.
Elementary analysis C, Found 48.32%; Calc. 48.5%; H Found 0.51%; Calc. 0.55%; N Found 14.0%; Calc. 14.1%.
19 Fnmr (CCl4 /DMSOd4) δ25.5 (d, JFF =9.35 Hz, 1F); 43.0 (d, JFF =19.6 Hz, 1F); 78.7 (dd, JFF =9.35 Hz, JFF =19.6 Hz, 1F).
1 Hnmr (CCl4 /DMSOd6) δ2.50 (S, 1H)
A 2.0 g amount of tetrafluoroisophthalonitrile was heated under reflux in 40 ml of methanol for 4 hours. The methanol was distilled off in vacuo to approximately one-fifth volume and ice water was then poured to the resultant mixture. The precipitated crystal was collected by filtration and was then washed with water and a small amount of cold methanol. After drying in vacuo, 1.6 g of the desired compound No. 20 was obtained.
The analytical results are as follows.
19 Fnmr (CCl4 /DMSOd6) δ24 (d, JFF =13 Hz, 1F); 38 (d, JFF =20 Hz, 1F); 75 (dd, JFF =20 Hz, JFF =13 Hz, 1F).
1 Hnmr (CCl4 /DMSOd6) δ4.3 (S, 3H).
The desired compound was obtained in the same manner as in Synthetic Example 5, except that ethanol was used in lieu of methanol. The yield was 90%.
The analytical results are as follows.
19 Fnmr (CCl4 /DMSOd6) δ22.7 (d, JFF =10.2 Hz, 1F); 32.7 (d, JFF =18.7 Hz, 1F); 75.2 (dd, JFF =18.7 Hz, JFF =10.1 Hz, 1F).
1 Hnmr (CCl4 /DMSOd6) δ1.5 (t, JHH =8 Hz, 3H); 4.7 (q, JHH =8 Hz, 2H).
The desired compound was obtained in the same manner as in Synthetic Example 5, except that isopropanol was used in lieu of methanol.
The yield was 86%.
A mixture of 2.0 g of isotetrafluorophthalonitrile, 1.0 g of phenol, and 3 g of potassium fluoride was heated under reflux for 1.5 hours in 30 ml of acetonitrile. After adding 40 ml of water, the reaction mixture was extracted with chloroform. After washing with water, the extract was dried with magnesium sulfate and the solvent was then distilled off to obtain 2.6 g of the residue. The crude product thus obtained was treated by silica gel chromatography (solvent:chloroform) to obtain 1.7 g (64% yield) of the desired compound in the form of crystal.
The analytical results are as follows.
19 Fnmr (CDl4 /DMSOd6) δ34.5 (d, JFF =12 Hz, 1F); 57.0 (d, JFF =18 Hz, 1F); 85.5 (dd, JFF =18 Hz, JFF =12 Hz, 1F).
1 Hnmr (CCl4 /DMSOd6) δ7-8 (m).
A solution of 1.2 g (10×10-3 mol) of 2,6-dimethylphenol in 40 ml of acetonitrile was dropwise added at a temperature of -10° C. to a solution of 2.0 g (10×10-3 mol) of tetrafluoroisophthalonitrile and 2.9 g (50×10-3 mol) of potassium fluoride. The mixture was allowed to stand at a temperature of -10° C. to 0° C. for 1 hour while stirring and the undissolved potassium fluoride was separated by filtration. The filtrate was concentrated to dryness in vacuo. The resultant residue was dissolved in a mixed solvent of acetone and cyclohexane and 2.3 g (77% yield) of the desired compound No. 37 was obtained as white crystal.
The analytical results are as follows.
19 F-NMR (acetone) δ26.0 (d, JFF =8.7 Hz, 1F); 41.0 (d, JFF =16.4 Hz, 1F); 80.0 (dd, JFF =8.7, 16.4 Hz, 1F).
1 H-NMR (CDCl3) δ2.15 (S, 6H); 6.95-7.1 (m, 3H).
A 2.0 g amount of tetrafluoroisophthalonitrile and 0.87 g of potassium fluoride were dissolved in 10 ml of acetonitrile. After cooling the mixture to a temperature of 0° C. by an ice-water bath, 1.1 g of phenyl mercaptan was dropwise added by a syringe. While mixture was maintained at a temperature of about 0° C., the mixture was stirred for 8 hours and the solvent was then distilled off. A 50 ml amount of water was added to the mixture and potassium fluoride was dissolved. The mixture was extracted with chloroform, and the extract was dried with magnesium sulfate. The chloroform was distilled off in vacuo and the resultant liquid was then distilled in vacuo to obtain 1.8 g (63% yield) of the desired compound No. 41 at a boiling point of 65° C. to 67° C./0.7 mmHg.
The analytical results are as follows.
19 Fnmr (CCl4 /DMSOd6) δ23.1 (d, JFF =11.9 Hz, 1F); 38.2 (d, JFF =18.9 Hz, 1F); 49.4(dd, JFF =18.9 Hz, 11.9 Hz, 1F).
1 Hnmr (CCl4 /DMSOd6) δ7.4 (S).
The mixture of 3.0 g of tetrafluoroisophthalonitrile, 1.2 g of β-methallyl alcohol and 1.8 g of potassium fluoride in 30 ml of acetonitrile was stirred at room temperature for 10 hours. The mixture was cooled and filtered. The filtrate was evaporated under reduced pressure. After 50 ml of water was added to the residue, the mixture was extracted with carbon tetrachloride, washed with water, and dried over sodium sulfate. After evaporating carbon tetrachloride, the residue of 2.9 g (crystal) was obtained.
The analytical results are as follows.
mp<50° C.
1 Hnmr (CDCl3) δ1.88 (3H, s), δ4.9-5.2 (H, m).
The desired compound was obtained in the same manner as in Synthetic Example 11, except that allyl alcohol was used in lieu of methallyl alcohol.
The analytical results are as follows.
19 Fnmr (CCl4 /DMSOd6) δ25.5 (d, JFF =9.0 Hz, 1F); 39.8 (d, JFF =18.4 Hz, 1F); 75.3 (m, 1F).
The mixture of 3.0 g tetrafluoroisophthalonitrile, 1.2 g of methyl cellosolve, and 1.8 g of potassium fluoride in 30 ml of acetonitrile was stirred at room temperature for 8 hours. The mixture was filtered. The filtrate was evaporated under reduced pressure. After 50 ml of water was added to the residue, the mixture was extracted with dichloromethane, washed with water, and dried over sodium sulfate. After evaporating dichloromethane, residue of 3.4 g was obtained. By column chromatography (Wakogel C-200; solvent-CH2 Cl2) pure oil (3.0 g) was isolated.
1 Hnmr (CDCl3) 3.38 (3H, s), 3.83 (2H, t, J=6 Hz), 4.63 (2H, m).
The mixture of 3.0 g of tetrafluoroisophthalonitrile, 1.7 g of furfuryl alcohol, and 1.8 g of potassium fluoride in 30 ml of acetonitrile was stirred at room temperature for 10 hours. The mixture was filtered. The filtrate was evaporated under reduced pressure. After 50 ml of water was added to the residue, the mixture was extracted with chloroform, washed with water and dried over magnesium sulfate. After evaporating chloroform, residue of 3.8 g was obtained. By column chromatography (florisil; solvent-chloroform) pure oil (3.2 g) was isolated.
A 5.0 g amount of tetrafluoroisophthalonitrile and 2.18 g of potassium fluoride were dissolved in 25 ml of acetonitrile, and 3.83 g of cyclohexanol was then dropwise added to the mixture. After the dropwise addition, the mixture was stirred at room temperature for 24 hours. The reaction mixture was filtered, the filtrate was concentrated in vacuo, and the concentrated liquid was poured to 50 ml of water. The resultant mixture was extracted with carbon tetrachloride. After washing with water, the extract was dried with anhydrous magnesium sulfate and the solvent was then distilled off. Thus, 6.2 g (88% yield) of the desired compound No. 47 was obtained.
The analytical results are as follows.
19 Fnmr (CDCl3).
δ: 26.0 (d, JFF =9.4 Hz, 1F); 41.0 (d, JFF =16.9 Hz, 1F); 75.5 (ddt, JFF =9.4 Hz, JFF =16.9 Hz, 1F).
A 3.0 g amount of tetrafluoroisophthalonitrile and 1.26 g of 20 ml acetonitrile were dissolved in 20 ml of acetonitrile. A 1.66 g amount of sec-butanol was dropwise added to the mixture and the mixture was then stirred at room temperature for 24 hours. After the mixture was filtered, the filtrate was concentrated in vacuo and the concentrated liquid was poured into 50 ml of water. The mixture was extracted with carbon tetrachloride. After washing with water, the resultant mixture was dried with anhydrous magnesium sulfate and the solvent was then distilled off. Thus, 3.4 g (89% yield) of the desired compound No. 48 was obtained.
The analytical results are as follows.
19 Fnmr (CDCl3).
δ: 23.7 (d, JFF =9.6 Hz, 1F); 38.7 (d, JFF =16.9 Hz, 1F); 74.3 (dd, JFF =16.9 Hz, JFF =9.6 Hz, 1F).
IR (KBr)
2250 cm-1 (C═N).
A 2.0 g amount of tetrafluoroisophthalonitrile and 0.87 g of potassium fluoride were dissolved in 10 ml of acetonitrile. After cooling the mixture to a temperature of 0° C., 0.76 g of n-propylmercaptan was gradually dropwise added to the mixture and the resultant mixture was stirred at a temperature of 0° C. or less for 12 hours. To the reaction mixture, 50 ml of water was added. The mixture was then extracted with chloroform. After washing with a saturated aqueous sodium bicarbonate solution, the mixture was dried with anhydrous magnesium sulfate. The chloroform was distilled off and the crude product was treated by silica gel column chromatography (solvent:n-hexane/ethyl acetate=3/1).
Thus, 1.7 g (66% yield) of the desired compound No. 52 was obtained. The analytical results are as follows.
19 Fnmr (CCl4).
δ: 22.0 (d, JFF =13.2 Hz, 1F); 38.7 (d, JFF =20.7 Hz, 1F); 51.7 (ddt, JFF =13.2 Hz, JFF =20.7 Hz, 1F).
The desired compound was prepared in the same manner as in Synthetic Example 17, except that the isopropylmercaptan was used in lieu of n-propylmercaptan. Thus, 1.6 g (63% yield) of the desired compound No. 51 was obtained.
The analytical results are as follows.
19 Fnmr (CCl4).
δ: 22.3 (d, JFF =13.0 Hz, 1F); 38.3 (d, JFF =20.2 Hz, 1F); 50.5 (ddt, JFF =13.0 Hz, JFF =20.2 Hz, 1F).
A 2.0 g amount of tetrafluoroisophthalonitrile and 0.87 g of potassium fluoride were dissolved in 10 ml of acetonitrile. After cooling to a temperature of 0° C., 0.90 g (1.04 ml) of n-butylmercaptan was gradually dropwise added to the mixture and the resultant mixture was stirred at a temperature of 0° C. or less for 12 hours. After 50 ml of water was added to the reaction mixture, the reaction mixture was extracted with chloroform and the extract was then washed with a saturated aqueous sodium bicarbonate solution, followed by drying with anhydrous magnesium sulfate. After distilling off the chloroform, the resultant crude product was distilled in vacuo. Thus, 2.08 g (77% yield) of the desired compound No. 52 was obtained.
The analytical results are as follows.
19 Fnmr (CCl4).
δ: 23.3 (d, JFF =14.1 Hz, 1F); 39.2 (d, JFF =21.4 Hz, 1F); 52.3 (ddt, JFF =14.1 Hz, JFF =21.4 Hz, 1F).
The desired compound was obtained in the same manner as in Synthetic Example 19, except that isobutylmercaptan was used in lieu of n-butylmercaptan.
Thus, 2.02 g (75% yield) of the desired compound was obtained.
The analytical results are as follows.
19 Fnmr (CCl4).
δ: 22.0 (d, JFF =11.3 Hz, 1F); 38.3 (d, JFF =18.8 Hz, 1F); 51.5 (ddt, HFF =11.3 Hz, JFF =18.8 Hz, 1F).
Powder germicides having the following compositions were prepared by mixing the ingredients listed below at room temperature.
______________________________________
Ingredient Parts by weight
______________________________________
Compound listed in Table 1
3
Clay 40
Talc 57
______________________________________
The powder germicides thus obtained were evaluated in the Test Examples below.
Wettable powder germicides having the following compositions were prepared by mixing the ingredients listed below at room temperature.
______________________________________
Ingredient Parts by weight
______________________________________
Compound listed in Table 1
75
Polyoxyethylele alkylallylether
9
White carbon 16
______________________________________
The wettable powder germicides thus obtained were evaluated in the Test Examples below.
Evaluation test of antibacterial and antifungal activity against pathogenic bacteria and fungi of plant
Conidia of pathogenic fungi and bacteria of plants cultivated on culture media were uniformly mixed in a PSA culture medium and a constant amount of the resultant mixture was poured into a vessel. Thus, uniform plates were prepared.
After solidifying, a filter paper having a diameter of 8 mm, which was prepared by absorbing a certain amount of the active compound, followed by air drying, was placed on the plate. After 48 hour incubation, the diameter of the inhibited circle was measured. Two tests were carried out in each run.
The results are shown in Table 2.
TABLE 2
______________________________________
Compound
Concentration
Diameter (mm) of Inhibited Circle
No. (a.i. ppm) B.c*.sup.1
A.k*.sup.1
P.o*.sup.1
X.c*.sup.1
______________________________________
1 500 0 0 30.5 16.8
2 " 0 0 14.3 15.0
3 " 0 0 14.0 22.5
4 " 0 17.3 19.8 20.0
5 " 0 0 15.5 13.3
6 " 0 0 22.5 13.8
7 " 0 0 10.2 0
8 " 0 0 15.5 0
9 " 31.5 0 30.8 0
10 " 0 0 10.2 0
11 " 31.0 0 18.5 30.0
12 " 30.8 14.5 34.3 0
13 " 0 0 10.2 0
14 " 22.5 22.5 34.3 0
15 " 0 0 13.3 0
16 " 0 0 11.5 0
17 " 0 10.2 10.2 0
18 " 0 0 10.2 0
19 11 31.2 0 33.7 0
20 500 38.9 29.0 35.2 28.0
21 " 33.0 13.4 19.8 30.5
22 " 30.2 31.5 21.5 16.4
23 " 31.5 32.3 30.2 30.4
24 " 33.5 33.5 34.1 30.5
25 " 32.1 31.5 33.0 31.5
26 " 15.0 30.5 29.0 28.0
27 " 30 30 34.8 28.8
28 " 22.5 29.0 30.5 28.2
29 " 29.8 30.5 33.0 0
30 " 17.0 12.5 12.3 0
31 " 30.3 17.7 24.5 10.0
32 " 18.0 12.5 13.8 11.0
33 " 20.0 13.8 15.0 12.3
34 " 20.5 15.0 15.5 11.8
35 " 20.0 19.2 15.5 12.5
36 " 18.0 16.0 16.0 0
37 " 13.5 0 13.5 10.0
38 " 22.5 13.2 14.0 0
39 " 19.8 12.5 12.2 0
40 " 21.3 13.8 15.3 0
42 " 30.0 33.5 34.1 29.2
43 " 28.5 30.8 32.8 22.5
44 " 27.8 29.2 30.5 19.8
45 " 19.8 22.5 21.5 28.0
46 " 13.5 15.8 18.3 0
47 " 31.0 33.2 32.5 29.0
48 " 14.8 30.0 28.0 27.5
49 " 30.2 15.5 31.5 10.0
50 " 30.0 30.5 28.2 29.8
51 " 32.2 31.0 32.5 28.8
52 " 30.0 29.8 30.5 28.0
53 " 15.0 28.2 27.0 26.0
54 " 15.0 28.8 28.0 26.8
Daconil*.sup.2
" 16.1 15.4 15.5 --
______________________________________
*.sup.1 B.c: Gray mold of vegetables
A.k: Black spot of pear
P.o: Blast of rice
X.c: Canker of citrus fruit
*.sup.2 Comparative test, available from SDS Biotech K.K.
A sample agent diluted to a certain concentration was uniformly sprayed on the developed leaves of pear trees (variety: Nijyusseiki) in an amount of 20 ml per 5 leaves and was dried in a room.
After air drying, conida of Alternaria kikuchiana formed on an apricot culture medium were sprayed on and was inoculated on the leaves. The incubation was carried out at a temperature of 25° C. and a relative humidity of 100% for 3 days. After 3 days, the infected area was measured. Five tests were carried out in each run.
The results are shown in Table 3.
TABLE 3
______________________________________
Compound
Concentration
Average infected
Controlled
No. (a.i. ppm) area (%) value (%)
______________________________________
1 500 0.3 99.7
2 " 0 100
3 " 5.3 94.7
6 " 0 100
7 " 10.0 90.0
12 " 5.6 94.4
20 " 15.0 85.0
23 " 5.1 94.9
24 " 3.2 96.8
25 " 41.0 59.0
26 " 65.0 35.0
28 " 28.5 71.5
Rovral*.sup.1
" 5.2 94.8
Control*.sup.2
-- 100 --
______________________________________
*.sup.1 Comparative test, available from RHONE POULENC
*.sup.2 No treatment
A sample liquid agent containing a certain amount of an active compound was uniformly sprayed on rice seedlings (variety: Jyukkoku) at true leaf stage in a pot with the volume of 200 liter/10 a and was air-dried in a green house.
After air drying, a spore suspension previously prepared in such a way that 40 conidia of rice blast fungus were present in a visual area of a 100 magnification microscope was uniformly sprayed and inoculated. Immediately, the sprayed rice seedlings were allowed to stand under dark conditions of a temperature of 23° C. and a relative humidity of 100%. After 48 hours, the rice seedlings were transferred to a green house and, after 10 days from the inocuration, the degree of the infection was determined. The inhibition value was calculated as follows. Three tests were carried out in each run. ##EQU1## wherein n: Number of leaves in each infection degree
f: index of refraction degree
N: Number of leaves examined
______________________________________
Index of infection
Number of lesion
degree per leaf
______________________________________
0 0
1 1-3
2 4-6
3 7-10
4 11 or more
______________________________________
The results are as shown in Table 4.
TABLE 4
__________________________________________________________________________
No. of leaves in
Concen- each infection
% of in-
Compound
tration
No. of leaves
degree fected
Infection
Chemical
No. (a.i. ppm)
examined
0 1 2 3 4 leaves
degree
injury
__________________________________________________________________________
38 500 185 163
19
3 0 0 13.5 3.4 --
Fujione*.sup.1
500 180 152
22
6 0 0 15.6 4.7 --
Control*.sup.2
-- 184 0 50
85 40 9 100 51.1 --
__________________________________________________________________________
*.sup.1 Comparative test, commercially available from NIPPON NOHYAKU K.K.
*.sup.2 No treatment
Test Example 3 was repeated except that the active compound was changed.
The results are as shown in Table 5.
TABLE 5
__________________________________________________________________________
No. of leaves in
Concen- each infection
% of in-
Compound
tration
No. of leaves
degree fected
Infection
Chemical
No. (a.i. ppm)
examined
0 1 2 3 4 leaves
degree
injury
__________________________________________________________________________
44 500 249 168
57 24
0
0 32.5 10.5 --
Fujione*.sup.1
500 280 190
70 10
10
0 32.1 10.7 --
Control*.sup.2
-- 270 20
110
90
40
10 92.6 41.7 --
__________________________________________________________________________
*.sup.1 Comparative test, commercially available from NIPPON NOHYAKU K.K.
*.sup.2 No treatment
A 10 ml amount of a potato-agar medium containing a certain concentration of each active ingredient was poured into a petri dish. After solidifying, a spore suspension of each test microorganism having 2.00 to 3.00×106 spores/ml was inoculated in the form of streaks with a platinum loop amount. The petri dish was allowed to stand in a constant temperature room at 25° C. for 3 days. Thereafter, the degree of growth was examined and the minimum inhibition concentration (i.e., "MIC") was determined. Four tests were carried out in each run.
The results are as shown in Table 6.
TABLE 6
______________________________________
MIC (ppm)
Compound Microorganism*.sup.1
No. A B C D E
______________________________________
14 <5 <5 50 50 >50
20 <5 <5 <5 5 10
21 <5 <5 <5 10 25
22 <5 <5 <5 <5 >50
23 <5 <5 <5 10 50
24 <5 <5 <5 10 25
25 <5 <5 <5 10 25
26 <5 <5 10 25 50
27 <5 <5 5 5 10
28 <5 <5 10 10 25
31 <5 <5 <5 10 >50
42 <5 <5 5 10 20
43 <5 <5 10 20 20
44 5 10 20 20 20
47 <5 <5 5 10 10
48 <5 <5 5 10 10
50 <5 <5 10 10 20
51 <5 <5 10 20 10
53 <5 <5 20 20 20
54 <5 5 20 20 20
Daconil*.sup.2
<5 50 10 5 >50
______________________________________
*.sup.1 A: Penicillium funiculosum
B: Aspergillus niger
C: Fusarium proliferatum
D: Gliocladium virens
E: Rhizopus storonifer
*.sup.2 Comparative test, available from SDS Biotech K.K.
A 10 ml amount of a potato-agar medium containing a certain concentration of each active ingredient was poured into a petri dish. After solidifying, the tip portion of the flora of each test microorganism previously incubated on a plate culture medium, which was punched with a 8 cmφ cork borer, was inoculated in the active ingredient containing culture medium. The culture medium thus obtained was allowed to stand in a constant temperature room at 28° C. for 3 days. Therefore, the growth of the microorganism was examined and the MIC was determined. Four tests were carried out in each run.
The results are as shown in Table 7.
TABLE 7
______________________________________
MIC (ppm)
Microorganism*.sup.1
Compound A B C D E
______________________________________
14 10 10 <50 10 10
20 5 5 10 10 10
21 5 10 10 10 10
22 25 25 25 10 25
23 5 10 10 10 <5
24 10 10 10 10 10
25 10 25 10 5 10
26 10 25 10 <5 <5
27 20 10 20 5 20
28 10 25 25 10 <5
31 10 50 25 25 25
42 20 20 10 10 10
43 20 100 50 20 10
44 20 20 50 20 20
47 20 20 50 10 10
48 20 10 20 5 10
50 20 20 20 20 20
51 20 50 20 10 20
53 20 50 50 20 20
54 20 50 50 20 50
Daconil*.sup.1
50 >50 50 50 >50
______________________________________
*.sup.1 See Remarks of Table 6
A 10 ml amount of a normal bouillon-agar culture medium was poured into a petri dish. After solidifying, a bacterial suspension previously obtained from the cultivation in the same liquid medium was inoculated in the form of streaks with a platinum loop amount. The petri dish was allowed to stand for 2 days in a constant temperature room at 30° C. Thereafter, the growth of the microorganism was examined and the MIC was determined. Four tests were carried out in each run.
The results are as shown in Table 8.
TABLE 8
______________________________________
MIC (ppm)
Microorganism*.sup.1
F G H I
______________________________________
Compound No. 14
<5 10 50 >50
Daconil*.sup.2 <5 10 >50 >50
______________________________________
*.sup.1 F: Bacillus subtilia
G: Staphylococcus aureus
H: Esherichia coli
I: Pseudomonas fluorescens
*.sup.2 Commercially available from SDS Biotech K.K.
For evaluation test of antibacterial action against bacterial soft rot disease of Japanese raddish the rhizome portion of Japanese raddish was cut to the form of a ring having a thickness of 1 cm with a 18 cmφ cork borer to form raddish chips. The chips were dipped in a liquid containing a certain concentration of an active ingredient for one hour. After air drying, one drop of a culture liquid containing bacterial soft rot bacteria which was cultivated at 27° C. for 24 hours in a normal bouillon medium by shaking culture, was inoculated in the center of the raddish chip. The raddish chip was allowed to stand at a temperature of 27° C. for 2 days under a high humidity condition. Therefore, the putrefaction degree of the raddish chip was examined. Five tests were carried out in each run.
The results are as shown in Table 9.
TABLE 9
______________________________________
Compound Concentration
No. (a.i., ppm) Degree of putrefaction*.sup.3
______________________________________
27 500 0
42 500 1
43 500 0
44 500 0
45 500 3
46 500 4
Copper 520 (as Cu) 2
hydroxide
Strepto- 200 0
mycin
______________________________________
*.sup.1 Commercially available from Sankyoh K.K.
*.sup.2 Commercially available from Meiji Seika K.K.
*.sup.3 Degree of Putrefaction
Putrefaction (%)
0 0
1 1-10
2 11-25
3 26-50
4 51-75
5 76-100
Claims (4)
1. A fluorinated isophthalonitrile compound having the general formula ##STR33## wherein Y is --O, --S, or --N(R'), R and R' are independently hydrogen, an alkyl group, an alkenyl group, an alkynyl group, a haloalkyl group, an alkoxyl group, an alkoxyalkyl group, a phenyl group which may be substituted, a tetrahydrofurfuryl group, or a cycloalkyl group, provided that, in the case of Y=--N(R'), R and R' or Y may be a heterocyclic compound residue.
2. A fluorinated isophthalonitrile compound as claimed in claim 1, wherein said compound is 2,4,5-trifluoro-6-methylamino-isophthalonitrile, 4-ethylamino-2,5,6-trifluoroisophthalonitrile, 4-diethylamino-2,5,6-trifluoroisophthalonitrile, 2,4,5-trifluoro-6-methoxyisophthalonitrile, 4-ethoxy-2,5,6-trifluoroisophthalonitrile, 2,4,5-trifluoro-6-propoxyisophthalonitrile, 2,4,5-trifluoro-6-isopoxyisophthalonitrile, 4-butoxy-2,5,6-trifluoroisophthalonitrile, 2,4,5-trifluoro-6-isobutoxyisophthalonitrile, 4-allyloxy-2,5,6-trifluoroisophthalonitrile, 2,4,5-trifluoro-6-methallyloxy-isophthalonitrile, 2,4,5-trifluoro-6-(2-methoxyethoxy)isophthalonitrile, 2,4,5-trifluoro-6-methylthioisophthalonitrile, 4-ethylthio-2,5,6-trifluoroisophthalonitrile, 2,4,5-trifluoro-6-propylthioisophthalonitrile, 2,4,5-trifluoro-6-isopropylthioisophthalonitrile, 4-butylthio-2,5,6-trifluoroisophthalonitrile, 2,4,5-trifluoro-6-isobutylthioisophthalonitrile, or 2,4,5-trifluoro-6-sec-butylthioisophthalonitrile.
3. A nonmedial fungicide comprising, as an effective ingredient, a fluorinated isophthalonitrile having the general formula ##STR34## wherein Y is --O, --S, or --N(R'), R and R' and independently hydrogen, an alkyl group, an alkenyl group, an alkynyl group, a haloalkyl group, an alkoxyl group, alkoxyalkyl group, a phenyl group which may be substituted, a tetrahydrofurfuryl group, or a cycloalkyl group, provided that, in the case of Y=--N(R'), R and R' or Y may be a heterocyclic compound residue.
4. A nonmedical fungicide as claimed in claim 3, wherein said fungicide contains 1% to 95% by weight of the fluorinate isophthalonitrile.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US06/770,481 US4614742A (en) | 1985-08-29 | 1985-08-29 | Fluorinated isophthalonitrile compound and nonmedical fungicide containing the same |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US06/770,481 US4614742A (en) | 1985-08-29 | 1985-08-29 | Fluorinated isophthalonitrile compound and nonmedical fungicide containing the same |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US4614742A true US4614742A (en) | 1986-09-30 |
Family
ID=25088692
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US06/770,481 Expired - Lifetime US4614742A (en) | 1985-08-29 | 1985-08-29 | Fluorinated isophthalonitrile compound and nonmedical fungicide containing the same |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US4614742A (en) |
Cited By (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO1990014338A1 (en) * | 1989-05-20 | 1990-11-29 | Fisons Plc | Anti-inflammatory 4-aminophenol derivatives |
| US5175336A (en) * | 1990-05-26 | 1992-12-29 | Bayer Aktiengesellschaft | Fluoromethylated polycyanobenzenes, their alkali metal cyanide adducts, processes for their preparation and use of the fluoromethylated polycyanobenzenes |
| CN102827034A (en) * | 2011-06-17 | 2012-12-19 | 中国中化股份有限公司 | P-dicyanoaniline-containing compounds and applications thereof |
| CN102827033A (en) * | 2011-06-17 | 2012-12-19 | 中国中化股份有限公司 | Compound containing o-dicyanoaniline and application thereof |
| CN102827071A (en) * | 2011-06-17 | 2012-12-19 | 中国中化股份有限公司 | Compound containing aminobenzonitrile and application thereof |
| WO2012171484A1 (en) | 2011-06-17 | 2012-12-20 | 中国中化股份有限公司 | Substituted cyanoaniline compounds, preparation and use thereof |
| CN106045880A (en) * | 2016-06-22 | 2016-10-26 | 云南大学 | N-halogenated aryl substituted chiral amino-acid ester compound as well as preparation method and application thereof |
Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3290353A (en) * | 1963-04-01 | 1966-12-06 | Diamond Alkali Co | Halogenated aromatic nitriles |
| US3637796A (en) * | 1968-10-30 | 1972-01-25 | Diamond Shamrock Corp | Trimesonitriles |
| US4069342A (en) * | 1973-12-12 | 1978-01-17 | Diamond Shamrock Corporation | Method for regulating rests using alkylthiotrichlorodicyanobenzenes |
| US4263206A (en) * | 1978-05-04 | 1981-04-21 | Imperial Chemical Industries Limited | Reactive dyestuffs containing chlorine or fluorine substituents and one or more 1,3-dicyanobenzene radicals linked to the dyestuff at the 2-, 4- or 6-position |
-
1985
- 1985-08-29 US US06/770,481 patent/US4614742A/en not_active Expired - Lifetime
Patent Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3290353A (en) * | 1963-04-01 | 1966-12-06 | Diamond Alkali Co | Halogenated aromatic nitriles |
| US3637796A (en) * | 1968-10-30 | 1972-01-25 | Diamond Shamrock Corp | Trimesonitriles |
| US4069342A (en) * | 1973-12-12 | 1978-01-17 | Diamond Shamrock Corporation | Method for regulating rests using alkylthiotrichlorodicyanobenzenes |
| US4263206A (en) * | 1978-05-04 | 1981-04-21 | Imperial Chemical Industries Limited | Reactive dyestuffs containing chlorine or fluorine substituents and one or more 1,3-dicyanobenzene radicals linked to the dyestuff at the 2-, 4- or 6-position |
Cited By (16)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO1990014338A1 (en) * | 1989-05-20 | 1990-11-29 | Fisons Plc | Anti-inflammatory 4-aminophenol derivatives |
| US5428044A (en) * | 1989-05-20 | 1995-06-27 | Fisons Plc | Anti-inflammatory 4-aminophenyl derivatives |
| US5175336A (en) * | 1990-05-26 | 1992-12-29 | Bayer Aktiengesellschaft | Fluoromethylated polycyanobenzenes, their alkali metal cyanide adducts, processes for their preparation and use of the fluoromethylated polycyanobenzenes |
| JP2014523414A (en) * | 2011-06-17 | 2014-09-11 | シノケム・コーポレーション | Substituted cyanoaniline compounds, their preparation and use |
| CN102827033A (en) * | 2011-06-17 | 2012-12-19 | 中国中化股份有限公司 | Compound containing o-dicyanoaniline and application thereof |
| CN102827071A (en) * | 2011-06-17 | 2012-12-19 | 中国中化股份有限公司 | Compound containing aminobenzonitrile and application thereof |
| WO2012171484A1 (en) | 2011-06-17 | 2012-12-20 | 中国中化股份有限公司 | Substituted cyanoaniline compounds, preparation and use thereof |
| CN103547565A (en) * | 2011-06-17 | 2014-01-29 | 中国中化股份有限公司 | Substituted cyanoaniline compounds, preparation and use thereof |
| CN102827034A (en) * | 2011-06-17 | 2012-12-19 | 中国中化股份有限公司 | P-dicyanoaniline-containing compounds and applications thereof |
| US8937072B2 (en) | 2011-06-17 | 2015-01-20 | Sinochem Corporation | Substituted cyanoaniline compounds, preparation and use thereof |
| CN102827071B (en) * | 2011-06-17 | 2015-02-25 | 中国中化股份有限公司 | Benzonitrile-substitute compound containing aminobenzonitrile and application cthereof |
| CN102827034B (en) * | 2011-06-17 | 2015-04-01 | 中国中化股份有限公司 | P-dicyanoaniline-containing compounds and applications thereof |
| CN102827033B (en) * | 2011-06-17 | 2015-04-01 | 中国中化股份有限公司 | Compound containing o-dicyanoaniline and application thereof |
| CN103547565B (en) * | 2011-06-17 | 2015-05-20 | 中国中化股份有限公司 | Substituted cyanoaniline compounds, preparation and use thereof |
| EP2757092A4 (en) * | 2011-06-17 | 2015-09-23 | Sinochem Corp | Substituted cyanoaniline compounds, preparation and use thereof |
| CN106045880A (en) * | 2016-06-22 | 2016-10-26 | 云南大学 | N-halogenated aryl substituted chiral amino-acid ester compound as well as preparation method and application thereof |
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